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  5. NDC Package Code: 83819-900-02 Dermveda Ultra Cold Sore Relief

NDC Package 83819-900-02 Dermveda Ultra Cold Sore Relief

Cardiospermum,Curcuma Longa Solution Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
83819-900-02
Package Description:
60 mL in 1 JAR
Product Code:
83819-900
Proprietary Name:
Dermveda Ultra Cold Sore Relief
Non-Proprietary Name:
Cardiospermum, Curcuma Longa
Substance Name:
Cardiospermum Halicacabum Flowering Top; Turmeric
Usage Information:
Do Not use on Children less than 2 YearsPlease perform a patch test for sensitive skin. Take a small amount with your finger and gently apply it on the affected area. Apply Liberally and use often till symptoms subside.
11-Digit NDC Billing Format:
83819090002
Product Type:
Human Otc Drug
Labeler Name:
Celcius Corp.
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
09-18-2024
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 83819-900-02?

The NDC Packaged Code 83819-900-02 is assigned to a package of 60 ml in 1 jar of Dermveda Ultra Cold Sore Relief, a human over the counter drug labeled by Celcius Corp.. The product's dosage form is solution and is administered via topical form.

Is NDC 83819-900 included in the NDC Directory?

Yes, Dermveda Ultra Cold Sore Relief with product code 83819-900 is active and included in the NDC Directory. The product was first marketed by Celcius Corp. on September 18, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 83819-900-02?

The 11-digit format is 83819090002. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-283819-900-025-4-283819-0900-02